Please choose an event type to view the corresponding MedsFacts report:

PYREXIA ( 17 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 10 FDA reports)
MALAISE ( 10 FDA reports)
BRONCHITIS ( 8 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 8 FDA reports)
INFECTION ( 8 FDA reports)
MYALGIA ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
RENAL FAILURE CHRONIC ( 6 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
CARDIAC TAMPONADE ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
ISCHAEMIC HEPATITIS ( 4 FDA reports)
NEPHROGENIC ANAEMIA ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HELICOBACTER TEST POSITIVE ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOCOMPLEMENTAEMIA ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
OCCULT BLOOD ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PUBIS FRACTURE ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DNA ANTIBODY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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